Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.41 (G)
Location

Chromosome 11:7008610 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs4468329, rs60892257

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2513 sample genotypes.

Variant displays